Peptides and peptidomimetic compounds, the manufacturing thereof as well as their use for preparing a therapeutically and/or preventively active pharmaceutical composition

ABSTRACT

Peptides, peptidomimetics and derivatives thereof of the general formula I: 
                         H 2 N-GHRPX 1 - β -X 4 X 5 X 6 X 7 X 8 X 9 X 10 -X 11  (I),               
in which
     X 1 -X 10  denote one of the 20 genetically coded amino acids, wherein X 8 , X 9  and X 10  may also denote a single chemical bond;   X 11  denotes OR 1  in which R 1  equals hydrogen or (C 1 -C 10 ) alkyl NR 2 R 3  with R 2  and R 3  are equal or different and denote hydrogen, (C 1 -C 10 ) alkyl, or
       a residue —W-PEG 5-60K , in which the PEG residue is attached via a suitable spacer W to the N-atom, or   a residue NH—Y—Z-PEG 5-60K , in which   Y denotes a chemical bond or a genetically coded amino acids from the group S, C, K or R and   Z denotes a spacer, via which a polyethylene glycol (PEG)-residue can be attached, and their physiologically acceptable salts, and   
       β denotes an amino acid, or a peptidomimetic element, which induces a bend or turn in the peptide backbone.

The present invention relates to peptides and peptidomimetic compounds, to the manufacturing thereof as well as to their use for preparing a therapeutically and/or preventively active drug and to such a pharmaceutical drug.

EP1586586 describes the use of peptides from the sequence of fibrin possessing anti-inflammatory effects.

Said effect may be based on the fact that the fibrin and fibrin fragments generated during the breakdown thereof bind to endothelial cells via its neo-N-terminus of the Bbeta-chain and to cells in the bloodstream via the sequence of the Aalpha-chain, thereby leading to the adhesion and transmigration of these cells into the tissue. The binding partner of the fibrin and fibrin fragments to the endothelial cells is the protein vascular endothelial (VE) cadherin, which is expressed exclusively in the adherens junction between neighboring endothelial cells. The peptides according to the invention block this interaction and thereby counteract the transmigration of blood cells. The natural defense against infections by the leukocytes in the blood is not adversely affected, however. Thus, the composition of the same, such as granulocytes, lymphocytes and monocytes, remains unaffected so that the natural defense process is maintained.

Fibrinogen is produced in the liver and, in this form, is biologically inactive and normally is provided in the blood at concentrations of around 3 g/l. Proteolytic cleavage of the proenzyme prothrombin results in the formation of thrombin, which cleaves off the fibrinopeptides A and B from the fibrinogen. In this way, fibrinogen is transformed into its biologically active form. Fibrin and fibrin cleavage products are generated.

Thrombin is formed whenever blood coagulation is activated, i.e. with damage to the tissue, be it of inflammatory, traumatic or degenerative genesis. The formation of fibrin as mediated by thrombin is basically a protective process aimed at quickly sealing any defects caused to the vascular system. However, the formation of fibrin also is a pathogenic process. The appearance of a fibrin thrombus as the triggering cause of cardiac infarction is one of the most prominent problems in human medicine.

The role which fibrin plays during the extravasation of inflammatory cells from the bloodstream into the tissue, which, on the one hand, is a desired process for the defense against pathogenic microorganisms or tumor cells in the tissue, but, on the other hand, is a process which, by itself, induces or prolongs damage done to the tissue, has so far not been examined at all or not to a sufficient extent. Fibrin binds to endothelial cells via its neo-N-terminus of Bbeta by means of the sequence to Bbeta and to cells in the bloodstream by means of the sequence Aalpha, thereby leading to the adhesion and transmigration of cells into the tissue.

By way of the mechanism described above the peptides or proteins according to the invention may prevent the adhesion of cells from the bloodstream to endothelial cells of the vascular wall and/or their subsequent transmigration from the blood into the tissue.

One of the principal abnormalities associated with acute inflammatory disease is the loss of endothelial barrier function. Structural and functional integrity of the endothelium is required for maintenance of barrier function and if either of these is compromised, solutes and excess plasma fluid leak through the monolayer, resulting in tissue oedema and migration of inflammatory cells. Many agents increase monolayer permeability by triggering endothelial cell shape changes such as contraction or retraction, leading to the formation of intercellular gaps (Lum & Malik, Am. J. Physiol. 267: L223-L241 (1994). These agents include e.g thrombin, bradykinin and vascular endothelial growth factor (VEGF).

Hyperpermeability of the blood vessel wall permits leakage of excess fluids and protein into the interstitial space. This acute inflammatory event is frequently allied with tissue ischemia and acute organ dysfunction. Thrombin formed at sites of activated endothelial cells (EC) initiates this microvessel barrier dysfunction due to the formation of large paracellular holes between adjacent EC (Carbajal et al, Am J Physiol Cell Physiol 279: C195-C204, 2000). This process features changes in EC shape due to myosin light chain phosphorylation (MLCP) that initiates the development of F-actin-dependent cytoskeletal contractile tension (Garcia et al, J Cell Physiol. 1995; 163:510-522 Lum & Malik, Am J Physiol Heart Circ Physiol. 273(5): H2442-H2451. (1997).

Thrombin-induced endothelial hyperpermeability may also be mediated by changes in cell-cell adhesion (Dejana J. Clin. Invest. 98: 1949-1953 (1996). Endothelial cell-cell adhesion is determined primarily by the function of vascular endothelial (VE) cadherin (cadherin 5), a Ca-dependent cell-cell adhesion molecule that forms adherens junctions. Cadherin 5 function is regulated from the cytoplasmic side through association with the accessory proteins b-catenin, plakoglobin (g-catenin), and p120 that are linked, in turn, to a-catenin (homologous to vinculin) and the F-actin cytoskeleton.

VE-cadherin has emerged as an adhesion molecule that plays fundamental roles in microvascular permeability and in the morphogenic and proliferative events associated with angiogenesis (Vincent et al, Am J Physiol Cell Physiol, 286(5): C987-C997 (2004). Like other cadherins, VE-cadherin mediates calcium-dependent, homophilic adhesion and functions as a plasma membrane attachment site for the cytoskeleton. However, VE-cadherin is integrated into signaling pathways and cellular systems uniquely important to the vascular endothelium. Recent advances in endothelial cell biology and physiology reveal properties of VE-cadherin that may be unique among members of the cadherin family of adhesion molecules. For these reasons, VE-cadherin represents a cadherin that is both prototypical of the cadherin family and yet unique in function and physiological relevance. A number of excellent reviews have addressed the contributions of VE-cadherin to vascular barrier function, angiogenesis, and cardiovascular physiology.

Evidence is accumulating that the VE-cadherin-mediated cell-cell adhesion is controlled by a dynamic balance between phosphorylation and dephosphorylation of the junctional proteins including cadherins and catenins. Increased tyrosine phosphorylation of b-catenin resulted in a dissociation of the catenin from cadherin and from the cytoskeleton, leading to a weak adherens junction (AJ). Similarly, tyrosine phosphorylation of VE-cadherin and b-catenin occurred in loose AJ and was notably reduced in tightly confluent monolayers (Tinsley et al., J Biol Chem, 274, 24930-24934 (1999).

In addition the correct clustering of VE-cadherin monomers in adherens junctions is indispensable for a correct signalling activity of VE-cadherin, since cell bearing a chimeric mutant (IL2-VE) containing a full-length VE-cadherin cytoplasmic tail is unable to cause a correct signalling despite its ability to bind to beta-catenin and p120 (Lampugnani et al, Mol. Biol. of the Cell, 13, 1175-1189 (2002).

Rho GTPases are a family of small GTPases with profound actions on the actin cytoskeleton of cells. With respect to the functioning of the vascular system they are involved in the regulation of cell shape, cell contraction, cell motility and cell adhesion. The three most prominent family members of the Rho GTPases are RhoA, Rac and cdc42. Activation of RhoA induces the formation of f-actin stress fibres in the cell, while Rac and cdc42 affect the actin cytoskeleton by inducing membrane ruffles and microspikes, respectively (Hall, Science, 279:509-514.1998). While Rac and cdc42 can affect MLCK activity to a limited extent via activation of protein PAK (Goeckeler et al. J. Biol. Chem., 275, 24, 18366-18374 (2000), RhoA has a prominent stimulatory effect on actin-myosin interaction by its ability to stabilize the phosphorylated state of MLC (Katoh et al., Am. J. Physiol. Cell. Physiol. 280, C1669-C1679 (2001). This occurs by activation of Rho kinase that in its turn inhibits the phosphatase PP1M that hydrolyses phosphorylated MLC. In addition, Rho kinase inhibits the actin-severing action of cofilin and thus stabilizes f-actin fibres (Toshima et al., Mol. Biol. of the Cell. 12, 1131-1145 (2001). Furthermore, Rho kinase can also be involved in anchoring the actin cytoskeleton to proteins in the plasma membrane and thus may potentially act on the interaction between junctional proteins and the actin cytoskeleton (Fukata et al. Cell Biol 145:347-361 (1999).

Thrombin can activate RhoA via Gα12/13 and a so-called guanine nucleotide exchange factor (GEF) (Seasholtz et al; Mol: Pharmacol. 55, 949-956 (1999). The GEF exchanges RhoA-bound GDP for GTP, by which RhoA becomes active. By this activation RhoA is translocated to the membrane, where it binds by its lipophilic geranyl-geranyl-anchor.

RhoA can be activated by a number of vasoactive agents, including lysophosphatidic acid, thrombin and endothelin. The membrane bound RhoA is dissociated from the membrane by the action of a guanine dissociation inhibitor (GDI) or after the action of a GTPase-activating protein (GAP). The guanine dissociation inhibitors (GDIs) are regulatory proteins that bind to the carboxyl terminus of RhoA.

GDIs inhibit the activity of RhoA by retarding the dissociation of GDP and detaching active RhoA from the plasma membrane. Thrombin directly activates RhoA in human endothelial cells and induces translocation of RhoA to the plasma membrane. Under the same conditions the related GTPase Rac was not activated. Specific inhibition of RhoA by C3 transferase from Clostridium botulinum reduced the thrombin-induced increase in endothelial MLC phosphorylation and permeability, but did not affect the transient histamine-dependent increase in permeability (van Nieuw Amerongen et al. Circ Res. 1998; 83:1115-11231 (1998). The effect of RhoA appears to be mediated via Rho kinase, because the specific Rho kinase inhibitor Y27632 similarly reduced thrombin-induced endothelial permeability.

Rac1 and RhoA have antagonistic effects on endothelial barrier function. Acute hypoxia inhibits Rac1 and activates RhoA in normal adult pulmonary artery endothelial cells (PAECs), which leads to a breakdown of barrier function (Wojciak-Stothard and Ridley, Vascul Pharmacol., 39:187-99 (2002). PAECs from piglets with chronic hypoxia induced pulmonary hypertension have a stable abnormal phenotype with a sustained reduction in Rac1 and an increase in RhoA activitity. These activities correlate with changes in the endothelial cytoskeleton, adherens junctions and permeability. Activation of Rac1 as well as inhibition of RhoA restored the abnormal phenotype and permeability to normal (Wojciak-Stothard et al., Am. J. Physiol, Lung Cell Mol. Physiol. 290, L1173-L1182 (2006).

Substances that active Rac1 and reduce RhoA activity to a level that is observed in endothelial cells in normal and stable conditions can therefore be expected to reduce endothelial hyperpermeability and have a beneficial therapeutic effect in a number of diseases. Preferably this effect is caused by a stabilization of the clustering of VE-cadherin in the adherens junction. An important component of the intracellular complex of proteins linked to VE-cadherin is fyn, a kinase which is a member of the src tyrosine kinases. The binding of the compounds which are subject to this invention to VE-cadherin cause a dissociation of fyn from VE-cadherin, which in turn leads to deactivation of thrombin induced active RhoA.

WO9216221 describes polypeptides which are covalently linked to long-chain polymers, as for instance methoxy-polyethylene glycol (PEG). The binding of polypeptides to such polymers frequently results in a prolongation of the biological half-life of these polypeptides and delays their renal excretion. A summary of these properties may be found in Davis et al., Polymeric Materials Pharmaceuticals for Biomedical Use, pp. 441-451 (1980) The addition of PEG-groups exerts this effect in a way proportional to the molecular weight of the PEGylated peptide, as, up to a certain size of the molecule, the glomular filtration rate is inversely proportional to the molecular weight.

WO2004/101600 also describes new poly(ethylene glycol)-modified compounds and their use, in particular with emphasis on modified peptides activating the erythropoietin receptor. Further examples for the covalent modification of peptides and proteins PEG residues are interleukins (Knauf et al., J. Biol. Chem. 1988, 263, 15064; Tsutumi et al., J. Controlled Release 1995, 33, 447), Interferons (Kita et al., Drug Delivery Res. 1990, 6 157), Catalase (Abuchowski et al., J. Biol. Chem. 1997, 252, 3582). A review of the prior art may be found in Reddy, Ann. of Pharmacotherapy, 2000, 34, 915.

A prolonged biological half-life is advantageous for various therapeutic uses of peptides. This is in particular true in cases of chronic diseases where the administration of the active agent over a prolonged period of time is indicated. With such indications this may improve the patient's compliance, as applying the active agent once a day will for instance be accepted more easily than continuous infusion. Apart from increasing the molecular mass by covalent modification, a prolongation of the persistency of polypeptides may be obtained by modifying them in such a way that their degradation by proteolytic enzymes (e.g. exo- or endoproteases or peptidases) is prevented.

Using various examples it has been shown that it is necessary to customize the appropriate modification for each peptide so as to prevent a significant influence on the pharmacodynamic effect as compared to the unmodified peptide. In this context the following may be referred to: Calcitonin (Lee et al. Pharm. Res. 1999, 16, 813), Growth Hormone Releasing Hormone (Esposito et al., Advanced Drug Delivery Reviews, 2003, 55, 1279), Glucagon like peptide 1 (Lee et al., Bioconjugate Res. 2005, 16, 377), as well as the growth hormone-receptor antagonist Pegvisomant (Ross et al., J. Clin. Endocrin. Metab. 2001, 86, 1716). The reviews by Caliceti and Veronese (Adv. Drug Deliv. Rev. 2003, 55 1261) and by Harris and Chess (Nature Rev. Drug Discovery 2003, 2, 214) discuss that in case of designing peptide- or protein-PEG-conjugates it is necessary to take into consideration the structure of the original substance, the molecular weight of the peptide and the polymer, the number of conjugated polymer chains as well as the linker chemistry, so as to obtain an effective peptide-PEG-conjugate.

Surprisingly it has now been found that peptides and peptidomimetics derived from the chain of the Bbeta(15-42)fibrin fragment, in which one or amino acids have been removed and which instead contain an amino acid or a peptidomimetic element promoting a bend or turn in the peptide backbone, as well as derivatives modified at the C-terminal end of the peptide sequence also have strong anti-inflammatory and endothelium stabilizing effects. The same applies to peptides, peptidomimetics and derivatives thereof, the modification of which prevents their destruction by proteases or peptidases, as well as to peptide-PEG-conjugates and peptidomimetic-PEG-conjugates generally derived from the basic sequence of the Bbeta(15-42)fibrin fragment containing such turn-inducing elements

Thus the invention relates peptidomimetics which are derived from the chain of the Bbeta(15-42)-fibrin fragment and wherein one or several of the amino acids of the sequence have been omitted and certain other amino acids residues of this chain substituted by genetically encoded or not genetically encoded amino acids or peptidomimetics, which have the property of inducing a bend or turn in the peptide backbone. They may exist as free peptides or may be modified at the C-terminal end and/or being linked to a polyethylene glycol (PEG)-polymer, and have anti-inflammatory and/or endothelium stabilizing effects. Esters or amides may for instance be taken into consideration as C-terminal derivatives.

The inventive compounds may have conservative substitutions of amino acids as compared to the natural sequence of fibrin of the warm blooded animals to be treated in one or several positions. A conservative substitution is defined as the side chain of the respective amino acid being replaced by a side chain of similar chemical structure and polarity, the side chain being derived from a genetically coded or not genetically coded amino acid. Families of amino acids of this kind having similar side chains are known in the art. They comprise for instance amino acids having basic side chains (lysins, arginins, histidine), acidic side chains (aspartic acid, glutamic acid), uncharged polar side chains (glycine, aspartamic acid, glutamine, serine, threonine, tyrosine, cysteine), non-polar side chains (alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (threonine, valine, isoleucine) and aromatic side chains (tyrosine, phenylalanine, tryptophane, histidine). Such conservative substitutions of side chains may preferably be carried out in non-essential positions. In this context, an essential position in the sequence is one wherein the side chain of the relevant amino acid is of significance for its biological effect.

The invention in particular concerns peptides, peptidomimetics and derivatives thereof of the following general formula I:

H₂N-GHRPX₁-β-X₄X₅X₆X₇X₈X₉X₁₀-X₁₁ (I), (SEQ ID NO: 1) in which

-   X₁-X₁₀ denote one of the 20 genetically coded amino acids, wherein     X₈, X₉ and X₁₀ individually or jointly may also denote a single     chemical bond and in which X₄ and X₅ may denote a suitable spacer of     a lengths similar to 2 amino acid residues and X₁ may also denote a     single chemical bond -   X₁₁ denotes OR₁ in which R₁ equals hydrogen or (C₁-C₁₀) alkyl, NR₂R₃     with R₂ and R₃ are equal or different and denote hydrogen, (C₁-C₁₀)     alkyl or a residue     -   —W-PEG_(5-60K), in which the PEG residue is attached via a         suitable spacer W to the N-atom, or     -   a residue     -   NH—Y—Z-PEG_(5-60K) ,     -   in which     -   Y denotes a single chemical bond or a genetically coded amino         acids from the group S, C, K or R and in which     -   Z denotes a spacer, via which a polyethylene glycol         (PEG)-residue can be attached, as well as their physiologically         acceptable salts,     -   and in which additionally -   β denotes an amino acid, whether genetically coded or not, or a     peptidomimetic element, which have the additional property of     inducing a bend or turn in the peptide backbone. Such amino acids     include without limitation L-proline, D-proline, L-hydroxyproline,     D-hydroxyproline, L-(O-benzyl)-hydroxyproline,     D-(O-benzyl)-hydroxyproline, L-(O -tert. butyl)-hydroxyproline,     4-(O-2-naphtyl)-hydroxyproline,     4-(O-2-naphtyl-methyl)-hydroxyproline, 4-(O-phenyl)-hydroxyproline,     4-(4-phenyl-benzyl)-proline, cis-3-phenyl-proline,     cis-4-phenyl-proline, trans-4-phenyl-proline, cis-5-phenyl-proline,     trans-5-phenyl-proline, 4-benzyl-proline, 4-bromobenzyl-proline,     4-cyclohexyl-proline, 4-fluor-proline,     L-tetrahydroisoquinoline-2-carboxylic acid (L-Tic), all     diastereomers of octahydro-indole-2-carboxylic acid (Oic), and all     diastereomers of 1-aza-bicyclo [3,3,0]octane-2-carboxylic acid.     Additional amino acids having the turn-inducing property are know to     one skilled in the art and are compounds of formula I containing     them also subject of this invention.

Peptidomimetic elements pertaining to this invention are residues, which are able to replace one or several amino acids of a peptide chain and which also have the additional property of inducing a bend or turn in the peptide backbone. Several such residues have for instance been described in the patent application WO2005/056577, in which they were used for the preparation of peptidic HIV inhibitors.

A selection of useful peptidomimetic elements for the purpose of this invention are, without limitation the following:

cis-2-aminocyclopentane carboxylic acid (cis-Acpc)

(1R,2R)-(2-aminocyclopentane carboxylic acid ((1R,2R)-Acpc)

(1S,2S)-(2-aminocyclopentane carboxylic acid ((1S,2S)-Acpc)

1-aminomethyl-cyclohexane acetic acid (1-Achc)

3-amino-1-carboxymethyl-pyridin-2-one (Acpo)

1-amino-cyclobutane-carboxylic acid (1-Acbc)

1-amino-cyclohexane-carboxylic acid (1-Achc)

cis-4-amino-cyclohexane-acetic acid (4-Acha)

(1R,2R)-2-aminocyclohexane carboxylic acid ((1R,2R)-Achc)

(1R,2S)-2-aminocyclohexane carboxylic acid ((1R,2S)-Achc)

(1S,2R)-2-aminocyclohexane carboxylic acid ((1S,2R)-Achc)

(1S,2S)-2-aminocyclohexane carboxylic acid ((1S,2S)-Achc)

1-amino-cyclopentane carboxylic acid (1-Acpec)

1-amino-cyclopropane carboxylic acid (1-Acprc)

4-(2-aminoethyl)-6-dibenzofuranpropionic acid (Aedfp)

(R,S)-1-aminoindane-1-carboxylic acid (1-Aic)

2-aminoindane-2-carboxylic acid (2-Aic)

2′-(aminomethyl)-biphenyl-2-carboxylic acid (Ambc)

2-aminomethyl-phenylacetic acid (Ampa)

3-amino-2-naphthoic acid (Anc)

4-amino-tetrahydropyran-4-carboxylic acid (Atpc)

(R,S)-2-aminotetraline-2-carboxylic acid (2-Atc)

(2S,6S,9S)-6-amino-2-carboxymethyl-3,8-diazabicyclo-[4,3,0]-nonane-1,4-dione (Acdn)

(R)-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (Acbt)

(S)-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one (Acbo)

(R,S)-3-amino-1-carboxymethyl-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one (1-Acmb)

(S)-4-amino-2-carboxymethyl-1,3,4,5-tetrahydro-2H-[2]-benzazepin-3-one (2-Acmb)

(R,S)-3-amino-1-carboxymethyl-valerolactame (Acmv)

3-(2-aminoethyl)-1-carboxymethyl-quinazoline-2,4-dione (Acq)

(2S,5S)-5-amino-1,2,4,5,6,7-hexahydro-azepino[3,2,1-hi]-indole-4-one-2-carboxylic acid (Haic)

(R,S)-3-amino-N-1-carboxymethyl-2-oxo-5-cyclohexyl-1,4-benzodiazepine (Accb)

(R,S)-3-amino-N-1-carboxymethyl-2-oxo-5-phenyl-1,4-benzodiazepine (Acpb)

(2S,11aS)-2-amino-10-carboxymethyl-1,2,3,11a-tetrahydro-10H-pyrrolo[2,1-c][1,4]-benzodiazepine-5,11-dione (PBD)

(2S,3′S)-2-(4′-(3′-benzyl-2′-oxo-piperazin-1-yl))-3-phenyl-propionic acid (Bppp)

3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (Cptd)

(R,S)-3-amino-9-Boc-1,2,3,4-tetrahydro-carbazole-3-carboxylic acid (Thc)

3-exo-amino-bicyclo[2.2.1]heptane-2-exo-carboxylic acid (Abhc)

(3S)-3-Amino-1-carboxymethyl-caprolactam (Accl)

(S,S)-(ProLeu)spirolactamePhe (PLSP)

2-Oxo-3-amino-7-thia-1-azabicyclo[4.3.0]nonane-9-carboxylich acid (BTD)

Preferred subject of this invention are compounds of the general formula I, in which:

-   X₁ denotes L, I, S, M or A, or a single, chemical bond -   X₄ denotes L, I, S, M or A, -   X₂ denotes E or D, -   X₃ denotes R or K -   X₅, X₆, X₇ denote A, G, S, or L -   X₄ and X₅ jointly denote a suitable spacer of a similar chain length     as 2 amino acid residues -   X₈ denotes G, A or L or a single chemical bond, -   X₉ denotes Y, F, H or a single chemical bond -   X₁₀ denotes R, K or a single chemical bond and in which -   β and X₁₁ have the meaning described above -   as well as their physiologically acceptable salts.

Especially preferred subject of this invention are compounds of the general formula II,

H₂N-GHRPX₁-β-X₄X₅GGX₈X₉X₁₀- X₁₁ (II), (SEQ ID NO: 2) in which

-   X₁ denotes either L, I, A or a single chemical bond -   X₄ denotes L, I, S, M or A, -   X₅ denote A, G, S, or L, or -   X₄ and X₅ jointly denote a suitable spacer of a similar chain length     as 2 amino acid residues, -   X₈, X₉, X₁₀ and X₁₁ have the meaning described above for formula I     and their physiologically acceptable salts.

Most highly preferred subjects of the invention are compounds of the general formula II, in which

-   X₁ denotes either L, I, A or a single chemical bond -   X₄ denotes I -   X₅ denotes S, -   X₁₁ denotes OH, OR₂ or NR₂R₃, where R₂ and R₃ are equal or different     and denote hydrogen or (C₁-C₁₀) alkyl, or a residue     C(NR₂R₃)—(S-succinimido)-(PEG_(5-40K)), in which the succinimide     residue is linked to the sulphur atom of the cysteine residue via     carbon atom 3 of the succinimide ring,     as well as their physiologically acceptable salts.

In the above formulas I and II the following letters represent amino acid residues in accordance with the general annotation for proteins and peptides: pPhenylalanine is F, leucine is L, isoleucine is I, methionine is M, valine is V, serine is S, proline is P, threonine is T, alanine is A, tyrosine is Y, histidine is H, glutamine is Q, asparagine is N, lysine is K, aspartic acid is D, glutamic acid is E, cysteine is C, tryptophan is W, arginine is R, glycine is G.

The amino acid residues in the compounds of Formula I may either be present in their D or their L configuration.

The term peptide refers to a polymer of these amino acids, which are linked via an amide linkage.

“Physiologically acceptable” means that salts are formed with acids or bases the addition of which does not have undesirable effects when used for humans. Preferable are salts with acids or bases the use of which is listed for use with warm blooded animals, in particular humans, in the US Pharmacopoeia or any other generally recognized pharmacopoeia.

PEG stands for a polyethylene glycol residue having a molecular weight of between 5.000 and 60.000 Dalton, this molecular weight being the maximum of a molecular weight distribution, so that individual components of the mixture may have a higher or lower molecular weight.

The invention furthermore concerns processes for the production of the peptides and peptide derivatives of general Formula (I), characterized in that, either

-   -   (A) the first amino acid at the C-terminal end of the respective         sequence is linked to a polymeric resin via a suitable cleavable         spacer, the subsequent amino acids or peptidomimetic elements,         optionally containing suitable protective groups for functional         groups, are linked step by step according to methods known in         the art, the finished peptide is cleaved off the polymeric resin         according to suitable methods known in the art, the protective         groups, if present, are cleaved off by suitable methods and the         peptide or peptide derivative is purified according to suitable         methods, or     -   (B) a PEG-group having a desired molecular weight is linked to a         polymeric resin via a suitable spacer, the first amino acid at         the N-terminal end of the peptide is linked using suitable         methods, the remaining steps being the same as described in (A),         or     -   (C) a lysine residue, containing a suitable protective group at         the ε-amino group is linked to a suitable polymeric resin via a         suitable spacer using suitable methods, the peptide chain is         synthesized as described in (A), following cleavage from the         polymeric resin and purification, if necessary, the protective         group at the ε-amino group is cleaved off using suitable         methods, a PEG group having a desired molecular weight is linked         to the ε-amino group using a suitable activated reagent, the         optionally remaining protective groups are cleaved off and the         final product is purified using suitable methods, or     -   (D) a peptide containing a cysteine residue is reacted with a         PEG-maleimide to form compounds of Formula (II).

Suitable processing steps following (A), (B) or (C) as well as suitable reagents are for instance described in document WO 2004/101600.

Embodiments of the respective processing steps are not new per se and will be clear to an experienced specialist in the field of organic synthesis.

Processes for linking a PEG-residue to a peptide chain will be known to the skilled artisan. For instance, a cysteine (C)-residue may be reacted with PEG-maleimide, resulting in a succinimide residue as spacer for residue Z. A further possibility is reacting an optionally activated C-terminal carboxy residue with an aminoalkyl-substituted PEG residue. A further possibility is the introduction of a PEG residue by reacting an aldehyde-substituted PEG residue with the ε-amino function of a lysine residue. Activated PEG reagents having suitable spacers and reactive groups may for instance be obtained from NOF Corporation (Tokyo, Japan).

The substances according to the invention and the use of the substances according to the invention for the production of a pharmaceutical drug are of particular significance for the production of a pharmaceutical drug for the therapy of diseases resulting from the tissue-damaging effect of white blood cells, or wherein the integrity and full physiological integrity of the layer of endothelial cells lining the blood vessels is impaired.

Diseases belonging to this group are those in context with autoimmunity, as for instance collagenosis, rheumatic diseases, inflammatory bowel diseases like Morbus Crohn or Colitis ulcerosa, psoriasis and psoriatic rheumatoid arthritis, and post/parainfectious diseases as well as diseases caused by a graft-versus-host reaction. A healing effect takes place as this medical drug blocks the migration of the white blood cells into the tissue. Thus the white blood cells remain in the blood stream and cannot cause an autoreactive effect harmful to the tissue. This effect of the inventive substances is furthermore important for the treatment of shock conditions, in particular in case of septic shock triggered by infection with gram-positive or gram-negative bacterial pathogens as well as viral infections and haemorrhagic shock caused by heavy loss of blood because of severe injuries or bacterial or viral infections.

The inventive substances may generally be used in situations that can be described with the terms “Systemic Inflammatory Response Syndrome (SIRS)”, “Acute Respiratory Distress Syndrome (ARDS)”, “Capillary Leak Syndrome (CLS)” and organ- or multiorgan failure, respectively.

Associated with a pharmaceutical drug for the therapy and/or prevention of rejection reactions of organ transplants there is a healing effect as this pharmaceutical drug prevents the migration of white blood cells from the blood stream into the donor organ, and the donor organ can therefore not be destroyed for instance by autoreactive lymphocytes.

Associated with a pharmaceutical drug for the therapy and/or prevention of arteriosclerosis there is a healing and/or preventive effect as this pharmaceutical drug blocks the migration of lymphocytes and monocytes into the wall of the tissue and thus the activation of the cells of the tissue wall. Thus the progress of arteriosclerosis is minimized or stopped, the progredience of arteriosclerotic plaque resulting therefrom is inhibited, causing the arteriosclerosis to recede.

Associated with a pharmaceutical drug for the therapy and/or prevention of reperfusion trauma following surgically or pharmaceutically induced re-supply with blood, e.g. following percutaneous coronary intervention, stroke, vessel surgery, cardiac bypass surgery and organ transplants, there is a healing and/or preventive effect as this pharmaceutical drug inhibits the migration of lymphocytes, neutrophils and monocytes into the wall of the vessel. Reperfusion trauma is caused by a lack of oxygen/acidosis of the cells of the vessel during its re-supply with blood, leading to their activation and/or damage. Because of this, lymphocytes, neutrophils and monocytes adhere to the vessel wall and migrate into it. Blocking the adherence and migration of lymphocytes, neutrophils and monocytes in the vessel wall causes the hypoxy/acidosis-induced damage to abate, without the subsequent inflammatory reaction causing a permanent damage to the vessel. The endothelium-stabilizing effect of the inventive compounds furthermore prevents the formation of oedemas as well as any further damage to the organs supplied via the respective blood vessels.

Associated with a pharmaceutical drug for the therapy and/or prevention of arteriosclerosis as a consequence of metabolic diseases or the process of aging, there is a healing and/or preventive effect as this pharmaceutical drug inhibits the migration of lymphocytes, neutrophils and monocytes into the vessel wall, thus inhibiting the progredience of arteriosclerotic plaque resulting therefrom.

The pharmaceutical drug according to the invention may also be used for the transportation of another drug. The inventive drug specifically binds a surface molecule on endothelial cells. Thus drugs linked thereto may be delivered to endothelial cells in high concentrations without any danger of them having side effects at other sites. An example that may be cited here is the use of substances inhibiting the division of cells, which, specifically brought to endothelial cells, may have an antiangiogenetic effect. This brings about a healing effect in tumor patients, as tumor growth is blocked by preventing the proliferation of endothelial cells and thus by preventing neoangiogenesis. The inventive compounds themselves may also develop an antiangiogenetic effect, as they, because of their endothelium-stabilizing effect, prevent the endothelial cells from changing into a proliferative phenotype and thus prevent the formation of new capillary blood vessels. Therefore they are themselves suitable for the treatment of all kinds of tumor diseases as well as the prevention and/or treatment of tumor metastases.

The inventive compounds of Formula (I) together with pharmaceutical adjuvants and additives, may be formulated into pharmaceutical preparations which also are a subject matter of the present invention. In order to prepare such formulations a therapeutically effective dose of the peptide or peptide derivative is mixed with pharmaceutically acceptable diluents, stabilizers, solubilizers, emulsifying aids, adjuvants or carriers and brought into a suitable therapeutic form. Such preparations for instance contain a dilution of various buffers (e.g. Tris-HCl, acetate, phosphate) of different pH and ionic strength, detergents and solubilizers (e.g. Tween 80, Polysorbat 80), antioxidants (e.g. ascorbic acid), and fillers (e.g. lactose, mannitol). These formulations may influence the biological availability and the metabolic behavior of the active agents.

The pharmaceutical preparations according to the invention may be administered orally, parenterally (intramuscularly, intraperitoneally, intravenously or subcutaneously), transdermally or in an erodible implant of a suitable biologically degradable polymer (e.g. polylactate or polyglycolate).

The effectiveness of the compounds according to this invention with respect to the prevention of RhoA activation and consequentially the change in the cytoskeletal structure of the endothelial cells may for instance be demonstrated by a method comprising the steps of:

-   -   a. contacting a confluent layer of cultured endothelial cells         with thrombin in the presence of at least one of the test         compounds     -   b. lysing the endothelial cells with a lysation buffer     -   c. measuring the RhoA activity with a specific assay,         preferentially a so-called “pull down assay”.

The effectiveness in vivo may for instance be established using a model of acute pulmonitis in a rodent. The acute pulmonitis is for instance caused in mice by the intratracheal instillation of bacterial lipopolysaccharide (LPS). The effect of the active substance is measured by measuring the amount of Evans' Blue injected into the animal in pulmonary lavage or by measuring the number of extravasated leukocytes in lung lavage fluid. The inventive compounds show an effect at a dose ranging from 0.001 mg/kg body weight to 500 mg/kg body weight, preferably at a dose ranging from 0.1 mg/kg to 50 mg/kg.

A further possibility for establishing the biological effect in vivo is the reduction or complete suppression of mortality because of an infection with haemolytic viruses or bacteria. For this purpose, mice are for instance infected with a dose of Dengue viruses, wherein 50% of the animals die within a period of 5-20 days after infection. The inventive compounds bring about a reduction of this mortality at a dose ranging from 0.001 to 500 mg/kg body weight, preferably at a dose ranging from 0.1 to 50 mg/g body weight.

The following examples serve to illustrate the invention without limiting it to the examples.

General Preparation and Purification of Peptides According to the Invention

The preparation and purification of the above peptide derivatives generally takes place by way of FMOC-strategy on acid-labile resin supports using a commercially available batch peptide synthesizer as also described in the literature (e.g. “solid phase peptide synthesis—A practical approach” by E. Atherton, R. C. Sheppard, Oxford University press 1989). N-alpha-FMOC-protected derivatives, the functional side-chains of which are protected by acid-sensitive protective groups, are used as amino acid components. Unless otherwise stated, purification is carried out by means of RP-chromatography using a water/acetonitrile gradient and 0.1% TFA as ion pair reagent.

EXAMPLE 1

Gly-His-Arg-Pro-(1S, 2R)Achc-Ile-Ser-Gly-Gly (SEQ ID NO: 3)

100 mg Tentagel (Rapp Polymere) with FMOC-Gly as the first amino acid of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.

The FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 μl DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3×900 μl 30% piperidine in DMF and thorough mixing for 4 minutes.

Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.

The amino acid derivatives FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-(1S,2R)-Achc, FMOC-Pro and FMOC-Ser(tBu) (NeoMPS) are employed.

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid. The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained Maldi-TOF, 909.05 m/z (m.i.).

EXAMPLE 2

Gly-His-Arg-Pro-Acdn-Ile-Ser-Gly-Gly (SEQ ID NO: 4)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Acdn, FMOC-Pro, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 989.05 m/z (m.i.).

EXAMPLE 3

Gly-His-Arg-Pro-(cis-4-Acha)-Ile-Ser-Gly-Gly (SEQ ID NO: 5)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Pro, FMOC-cis-4-Acha, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, m/z 929.05 (m.i.).

EXAMPLE 4

Gly-His-Arg-Pro-Haic-Ile-Ser-Gly-Gly (SEQ ID NO: 6)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Pro, FMOC-Haic, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 998.10 m/z (m.i.).

EXAMPLE 5

Gly-His-Arg-Pro-Leu-(1S, 2R)Achc-Ile-Ser-Gly-Gly (SEQ ID NO: 7)

100 mg Tentagel (Rapp Polymere) with FMOC-Gly as the first amino acid of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.

The FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 μl DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3×900 μl 30% piperidine in DMF and thorough mixing for 4 minutes.

Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.

The amino acid derivatives FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Leu, FMOC-Ile, FMOC-(1S,2R)-Achc, FMOC-Pro and FMOC-Ser(tBu) (NeoMPS) are employed.

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid. The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained Maldi-TOF, 1023.67 m/z (m.i.).

EXAMPLE 6

Gly-His-Arg-Pro-Leu-Acdn-Ile-Ser-Gly-Gly (SEQ ID NO: 8)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Acdn, FMOC-Pro, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 1103.67 m/z (m.i.).

EXAMPLE 7

Gly-His-Arg-Pro-Leu-(cis-4-Acha)-Ile-Ser-Gly-Gly (SEQ ID NO: 9)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Leu, FMOC-Ile, FMOC-Pro, FMOC-cis-4-Acha, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 1043.22 m/z (m.i.).

EXAMPLE 8

Gly-His-Arg-Pro-Leu-Haic-Ile-Ser-Gly-Gly (SEQ ID NO: 10)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Pro, FMOC-Haic, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 1112.27 m/z (m.i.).

EXAMPLE 9

Gly-His-Arg-Pro-Ala-(1S, 2R)Achc-Ile-Ser-Gly-Gly (SEQ ID NO: 11)

100 mg Tentagel (Rapp Polymere) with FMOC-Gly as the first amino acid of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.

The FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 μl DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3×900 μl 30% piperidine in DMF and thorough mixing for 4 minutes.

Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.

The amino acid derivatives FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ala, FMOC-Ile, FMOC-(1S,2R)-Achc, FMOC-Pro and FMOC-Ser(tBu) (NeoMPS) are employed.

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained Maldi-TOF, 981.14 m/z (m.i.).

EXAMPLE 10

Gly-His-Arg-Pro-Ala-Acdn-Ile-Ser-Gly-Gly (SEQ ID NO: 12)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Ala, FMOC-Acdn, FMOC-Pro, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 1061.14 m/z (m.i.).

EXAMPLE 11

Gly-His-Arg-Pro-Ile-(cis-4-Acha)-Ile-Ser-Gly-Gly (SEQ ID NO: 13)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Pro, FMOC-cis-4-Acha, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 1043.28 m/z (m.i.).

EXAMPLE 12

Gly-His-Arg-Pro-Ile-Haic-Ile-Ser-Gly-Gly (SEQ ID NO: 14)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Pro, FMOC-Haic, FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 1112.41 m/z (m.i.).

The following peptides peptidomimetics were prepared following the general procedure described in Example 1 above, using the appropriate protected building blocks:

Gly-His-Arg-Pro-Leu-Pro-Ile-Ser-Gly-Gly (SEQ ID NO: 15) Gly-His-Arg-Pro-Leu-D-Pro-Ile-Ser-Gly-Gly Gly-His-Arg-Pro-Leu-L-hydroxyproline-Ile-Ser-Gly- Gly (SEQ ID NO: 16) Gly-His-Arg-Pro-Leu-D-hydroxproline-Ile-Ser-Gly- Gly Gly-His-Arg-Pro-Leu-L-(O-benzyl-hydroxyproline)- Ile-Ser-Gly-Gly (SEQ ID NO: 17) Gly-His-Arg-Pro-Leu-D-(O-benzyl-hydroxyproline)- Ile-Ser-Gly-Gly Gly-His-Arg-Pro-Leu-L-(O-t-butyl-hydroxyproline)- Ile-Ser-Gly-Gly (SEQ ID NO: 18) Gly-His-Arg-Pro-Leu-L-(O-2-naphtyl-hydroxy- proline)-Ile-Ser-Gly-Gly (SEQ ID NO: 19) Gly-His-Arg-Pro-Leu-L-(O-2-naphtyl-methyl-hydroxy- proline)-Ile-Ser-Gly-Gly (SEQ ID NO: 20) Gly-His-Arg-Pro-Leu-L-(O-phenyl-hydroxyproline)- Ile-Ser-Gly-Gly (SEQ ID NO: 21) Gly-His-Arg-Pro-Leu-L-4-(4-pheny-benzyl-proline)- Ile-Ser-Gly-Gly (SEQ ID NO: 22) Gly-His-Arg-Pro-Leu-L-(cis-3-phenyl-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 23) Gly-His-Arg-Pro-Leu-L-(cis-4-phenyl-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 24) Gly-His-Arg-Pro-Leu-L-(trans-4-phenyl-proline)- Ile-Ser-Gly-Gly (SEQ ID NO: 25) Gly-His-Arg-Pro-Leu-L-(cis-5-phenyl-proline)-Ile- Ser-Gly-Gly-Gly (SEQ ID NO: 26) Gly-His-Arg-Pro-Leu-L-(trans-5-phenyl-proline)- Ile-Ser-Gly-Gly (SEQ ID NO: 27) Gly-His-Arg-Pro-Leu-L-(4-benzyl-proline)-Ile-Ser- Gly-Gly (SEQ ID NO: 28) Gly-His-Arg-Pro-Leu-L-(4-(4-bromobenzyl)-proline)- Ile-Ser-Gly-Gly (SEQ ID NO: 29) Gly-His-Arg-Pro-Leu-L-(4-cyclohexyl-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 30) Gly-His-Arg-Pro-Leu-L-(4-fluoro-proline)-Ile-Ser- Gly-Gly (SEQ ID NO: 31) Gly-His-Arg-Pro-Leu-L-Tic-Ile-Ser-Gly-Gly (SEQ ID NO: 32) Gly-His-Arg-Pro-Leu-(SSS)-Oic-Ile-Ser-Gly-Gly (SEQ ID NO: 33) Gly-His-Arg-Pro-Leu-(SSS)1-aza-bicyclo[3.3.0] bicyclooctan-carboxyl-Ile-Ser-Gly-Gly  (SEQ ID NO: 34) Gly-His-Arg-Pro-Leu-cis-Acpc-Ile-Ser-Gly-Gly (SEQ ID NO: 35) Gly-His-Arg-Pro-Leu-(1R, 2R)-Acpc-Ile-Ser-Gly-Gly (SEQ ID NO: 36) Gly-His-Arg-Pro-Leu-(1S, 2S)-Acpc-Ile-Ser-Gly-Gly (SEQ ID NO: 37) Gly-His-Arg-Pro-Leu-(1-Acha)-Ile-Ser-Gly-Gly (SEQ ID NO: 38) Gly-His-Arg-Pro-Leu-Acpo-Ile-Ser-Gly-Gly (SEQ ID NO: 39) Gly-His-Arg-Pro-Leu-(1-Acbc)-Ile-Ser-Gly-Gly (SEQ ID NO: 40) Gly-His-Arg-Pro-Leu-Acpo-Ile-Ser-Gly-Gly (SEQ ID NO: 41) Gly-His-Arg-Pro-Leu-(1-Achc)-Ile-Ser-Gly-Gly (SEQ ID NO: 42) Gly-His-Arg-Pro-Leu-((1R, 2S)-2-Achc)-Ile-Ser-Gly- Gly (SEQ ID NO: 43) Gly-His-Arg-Pro-Leu-((1S, 2R)-2-Achc)-Ile-Ser-Gly- Gly (SEQ ID NO: 44) Gly-His-Arg-Pro-Leu-((1S, 2S)-2-Achc)-Ile-Ser-Gly- Gly (SEQ ID NO: 45) Gly-His-Arg-Pro-Leu-(1-Acpec)-Ile-Ser-Gly-Gly (SEQ ID NO: 46) Gly-His-Arg-Pro-Leu-(1-Acprc)-Ile-Ser-Gly-Gly (SEQ ID NO: 47) Gly-His-Arg-Pro-Leu-Aedfp-Ile-Ser-Gly-Gly (SEQ ID NO: 48) Gly-His-Arg-Pro-Leu-(1-Aic)-Ile-Ser-Gly-Gly (SEQ ID NO: 49) Gly-His-Arg-Pro-Leu-(2-Aic)-Ile-Ser-Gly-Gly (SEQ ID NO: 50) Gly-His-Arg-Pro-Leu-Ambc-Ile-Ser-Gly-Gly (SEQ ID NO: 51) Gly-His-Arg-Pro-Leu-Ampa-Ile-Ser-Gly-Gly (SEQ ID NO: 52) Gly-His-Arg-Pro-Leu-Anc-Ile-Ser-Gly-Gly (SEQ ID NO: 53) Gly-His-Arg-Pro-Leu-Atpc-Ile-Ser-Gly-Gly (SEQ ID NO: 54) Gly-His-Arg-Pro-Leu-(2-Atc)-Ile-Ser-Gly-Gly (SEQ ID NO: 55) Gly-His-Arg-Pro-Leu-Acbt-Ile-Ser-Gly-Gly (SEQ ID NO: 56) Gly-His-Arg-Pro-Leu-Acbo-Ile-Ser-Gly-Gly (SEQ ID NO: 57) Gly-His-Arg-Pro-Leu-(1-Acmb)-Ile-Ser-Gly-Gly (SEQ ID NO: 58) Gly-His-Arg-Pro-Leu-(2-Acmb)-Ile-Ser-Gly-Gly (SEQ ID NO: 59) Gly-His-Arg-Pro-Leu-Acmv-Ile-Ser-Gly-Gly (SEQ ID NO: 60) Gly-His-Arg-Pro-Leu-Acq-Ile-Ser-Gly-Gly (SEQ ID NO: 61) Gly-His-Arg-Pro-Leu-Accb-Ile-Ser-Gly-Gly (SEQ ID NO: 62) Gly-His-Arg-Pro-Leu-Acpb-Ile-Ser-Gly-Gly (SEQ ID NO: 63) Gly-His-Arg-Pro-Leu-PBD-Ile-Ser-Gly-Gly (SEQ ID NO: 64) Gly-His-Arg-Pro-Leu-ppp-Ile-Ser-Gly-Gly (SEQ ID NO: 65) Gly-His-Arg-Pro-Leu-Cptd-Ile-Ser-Gly-Gly (SEQ ID NO: 66) Gly-His-Arg-Pro-Leu-Thc-Ile-Ser-Gly-Gly (SEQ ID NO: 67) Gly-His-Arg-Pro-Leu-bhc-Ile-Ser-Gly-Gly (SEQ ID NO: 68) Gly-His-Arg-Pro-Leu-Accl-Ile-Ser-Gly-Gly (SEQ ID NO: 69) Gly-His-Arg-Pro-Leu-PLSP-Ile-Ser-Gly-Gly (SEQ ID NO: 70) Gly-His-Arg-Pro-Leu-BTD-Ile-Ser-Gly-Gly (SEQ ID NO: 71) Gly-His-Arg-Pro-Pro-Ile-Ser-Gly-Gly- (SEQ ID NO: 72) Gly-His-Arg-Pro-D-Pro-Ile-Ser-Gly-Gly Gly-His-Arg-Pro-L-hydroxyproline-Ile-Ser-Gly-Gly (SEQ ID NO: 73) Gly-His-Arg-Pro-D-hydroxproline-Ile-Ser-Gly-Gly Gly-His-Arg-Pro-L-(O-benzyl-hydroxyproline)-Ile- Ser-Gly-Gly (SEQ ID NO: 74) Gly-His-Arg-Pro-D-(O-benzyl-hydroxyproline)-Ile- Ser-Gly-Gly Gly-His-Arg-Pro-L-(O-t-butyl-hydroxyproline)-Ile- Ser-Gly-Gly (SEQ ID NO: 75) Gly-His-Arg-Pro-L-(O-2-naphtyl-hydroxyproline)- Ile-Ser-Gly-Gly (SEQ ID NO: 76) Gly-His-Arg-Pro-L-(O-2-naphtyl-methyl-hydroxy- proline)-Ile-Ser-Gly-Gly (SEQ ID NO: 77) Gly-His-Arg-Pro-L-(O-phenyl-hydroxyproline)-Ile- Ser-Gly-Gly (SEQ ID NO: 78) Gly-His-Arg-Pro-L-4-(4-pheny-benzyl-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 79) Gly-His-Arg-Pro-L-(cis-3-phenyl-proline)-Ile-Ser- Gly-Gly (SEQ ID NO: 80) Gly-His-Arg-Pro-L-(cis-4-phenyl-proline)-Ile-Ser- Gly-Gly (SEQ ID NO: 81) Gly-His-Arg-Pro-L-(trans-4-phenyl-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 82) Gly-His-Arg-Pro-L-(cis-5-phenyl-proline)-Ile-Ser- Gly-Gly (SEQ ID NO: 83) Gly-His-Arg-Pro-L-(trans-5-phenyl-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 84) Gly-His-Arg-Pro-L-(4-benzyl-proline)-Ile-Ser-Gly- Gly (SEQ ID NO: 85) Gly-His-Arg-Pro-L-(4-(4-bromobenzyl)-proline)-Ile- Ser-Gly-Gly (SEQ ID NO: 86) Gly-His-Arg-Pro-L-(4-cyclohexyl-proline)-Ile-Ser- Gly-Gly (SEQ ID NO: 87) Gly-His-Arg-Pro-L-(4-fluoro-proline)-Ile-Ser-Gly- Gly (SEQ ID NO: 88) Gly-His-Arg-Pro-L-Tic-Ile-Ser-Gly-Gly (SEQ ID NO: 89) Gly-His-Arg-Pro-(SSS)-Oic-Ile-Ser-Gly-Gly (SEQ ID NO: 90) Gly-His-Arg-Pro-(SSS)1-aza-bicyclo[3.3.0]bicyclo- octan-carboxyl-Ile-Ser-Gly-Gly (SEQ ID NO: 91) Gly-His-Arg-Pro-cis-Acpc-Ile-Ser-Gly-Gly (SEQ ID NO: 92) Gly-His-Arg-Pro-(1R, 2R)-Acpc-Ile-Ser-Gly-Gly (SEQ ID NO: 93) Gly-His-Arg-Pro-(1S, 2S)-Acpc-Ile-Ser-Gly-Gly (SEQ ID NO: 94) Gly-His-Arg-Pro-(1-Acha)-Ile-Ser-Gly-Gly (SEQ ID NO: 95) Gly-His-Arg-Pro-Acpo-Ile-Ser-Gly-Gly (SEQ ID NO: 96) Gly-His-Arg-Pro-(1-Acbc)-Ile-Ser-Gly-Gly (SEQ ID NO: 97) Gly-His-Arg-Pro-Acpo-Ile-Ser-Gly-Gly- (SEQ ID NO: 98) Gly-His-Arg-Pro-(1-Achc)-Ile-Ser-Gly-Gly (SEQ ID NO: 99) Gly-His-Arg-Pro-((1R, 2S)-2-Achc)-Ile-Ser-Gly-Gly (SEQ ID NO: 100) Gly-His-Arg-Pro-((1S ,2R)-2-Achc)-Ile-Ser-Gly-Gly (SEQ ID NO: 101) Gly-His-Arg-Pro-((1S ,2S)-2-Achc)-Ile-Ser-Gly-Gly (SEQ ID NO: 102) Gly-His-Arg-Pro-(1-Acpec)-Ile-Ser-Gly-Gly (SEQ ID NO: 103) Gly-His-Arg-Pro-(1-Acprc)-Ile-Ser-Gly-Gly (SEQ ID NO: 104) Gly-His-Arg-Pro-Aedfp-I1e-Ser-Gly-Gly (SEQ ID NO: 105) Gly-His-Arg-Pro-(1-Aic)-Ile-Ser-Gly-Gly (SEQ ID NO: 106) Gly-His-Arg-Pro-(2-Aic)-Ile-Ser-Gly-Gly (SEQ ID NO: 107) Gly-His-Arg-Pro-Ambc-Ile-Ser-Gly-Gly (SEQ ID NO: 108) Gly-His-Arg-Pro-Ampa-Ile-Ser-Gly-Gly (SEQ ID NO: 109) Gly-His-Arg-Pro-Leu-Asp-Lys-Anc-Ile-Ser-Gly-Gly (SEQ ID NO: 110) Gly-His-Arg-Pro-Atpc-Ile-Ser-Gly-Gly (SEQ ID NO: 111) Gly-His-Arg-Pro-(2-Atc)-Ile-Ser-Gly-Gly (SEQ ID NO: 112) Gly-His-Arg-Pro-Acbt-Ile-Ser-Gly-Gly (SEQ ID NO: 113) Gly-His-Arg-Pro-Acbo-Ile-Ser-Gly-Gly (SEQ ID NO: 114) Gly-His-Arg-Pro-(1-Acmb)-Ile-Ser-Gly-Gly (SEQ ID NO: 115) Gly-His-Arg-Pro-(2-Acmb)-Ile-Ser-Gly-Gly (SEQ ID NO: 116) Gly-His-Arg-Pro-Acmv-Ile-Ser-Gly-Gly (SEQ ID NO: 117) Gly-His-Arg-Pro-Acq-Ile-Ser-Gly-Gly (SEQ ID NO: 118) Gly-His-Arg-Pro-Accb-Ile-Ser-Gly-Gly (SEQ ID NO: 119) Gly-His-Arg-Pro-Acpb-Ile-Ser-Gly-Gly (SEQ ID NO: 120) Gly-His-Arg-Pro-PBD-Ile-Ser-Gly-Gly (SEQ ID NO: 121) Gly-His-Arg-Pro-Bppp-Ile-Ser-Gly-Gly (SEQ ID NO: 122) Gly-His-Arg-Pro-Cptd-Ile-Ser-Gly-Gly (SEQ ID NO: 123) Gly-His-Arg-Pro-Thc-Ile-Ser-Gly-Gly (SEQ ID NO: 124) Gly-His-Arg-Pro-Abhc-Ile-Ser-Gly-Gly (SEQ ID NO: 125) Gly-His-Arg-Pro-Accl-Ile-Ser-Gly-Gly (SEQ ID NO: 126) Gly-His-Arg-Pro-PLSP-Ile-Ser-Gly-Gly (SEQ ID NO: 127) Gly-His-Arg-Pro-BTD-Ile-Ser-Gly-Gly (SEQ ID NO: 128)

EXAMPLE 13

Gly-His-Arg-Pro-(1S, 2R)Achc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 129)

100 mg Tentagel-S-RAM (Rapp-Polymere) at a load of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.

The FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 μl DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3×900 μl 30% piperidine in DMF and thorough mixing for 4 minutes.

Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.

The amino acid derivatives FMOC-Arg(Pbf), FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-(1S,2R)-Achc, and FMOC-Ser(tBu) (NeoMPS) are employed.

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained, Molecular weight by mass spectrometry: 908.08 (MALDI-TOF)

EXAMPLE 14

Gly-His-Arg-Pro-Leu-Acdn-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 130)

The solid phase synthesis of this compound was done according to the description in example 1; the amino acid and peptidomimetic derivatives employed in the coupling steps were: FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Acdn, and FMOC-Ser(tBu) (NeoMPS).

When synthesis is completed the peptide resin is dried. The peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature. By way of filtration, concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.

The peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 μm in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm. The purity of the individual fractions is determined by analyt. RP-HPLC and mass spectrometry. Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained. Maldi-TOF, 998.01 m/z (m.i.).

The following peptides peptidomimetics were prepared following the general procedure described in Example 1 above, using the appropriate protected building blocks:

Gly-His-Arg-Pro-Pro-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 131) Gly-His-Arg-Pro-D-Pro-Ile-Ser-Gly-Gly-NH₂ Gly-His-Arg-Pro-L-hydroxyproline-Ile-Ser-Gly-Gly- NH₂ (SEQ ID NO: 132)  Gly-His-Arg-Pro-Leu-D-hydroxproline-Ile-Ser-Gly- Gly-NH₂ Gly-His-Arg-Pro-Leu-L-(O-benzyl-hydroxyproline)- Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 133) Gly-His-Arg-Pro-D-(O-benzyl-hydroxyproline)-Ile- Ser-Gly-Gly-NH₂ Gly-His-Arg-Pro-Leu-L-(O-t-butyl-hydroxyproline)- Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 134) Gly-His-Arg-Pro-L-(O-2-naphtyl-hydroxyproline)- Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 135) Gly-His-Arg-Pro-L-(O-2-naphtyl-methyl-hydroxy- proline)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 136) Gly-His-Arg-Pro-Leu-L-(O-phenyl-hydroxyproline)- Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 137) Gly-His-Arg-Pro-4-(4-pheny-benzyl-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 138) Gly-His-Arg-Pro-L-(cis-3-phenyl-proline)-Ile-Ser- Gly-Gly-NH₂ (SEQ ID NO: 139) Gly-His-Arg-Pro-Leu-L-(cis-4-phenyl-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 140) Gly-His-Arg-Pro-L-(trans-4-phenyl-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 141) Gly-His-Arg-Pro-Leu-L-(cis-5-phenyl-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 142) Gly-His-Arg-Pro-L-(trans-5-phenyl-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 143) Gly-His-Arg-Pro-L-(4-benzyl-proline)-Ile-Ser-Gly- Gly-NH₂ (SEQ ID NO: 144) Gly-His-Arg-Pro-L-(4-(4-bromobenzyl)-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 145) Gly-His-Arg-Pro-Ala-L-(4-cyclohexyl-proline)-Ile- Ser-Gly-Gly-NH₂ (SEQ ID NO: 146) Gly-His-Arg-Pro-Ile-L-(4-fluoro-proline)-Ile-Ser- Gly-Gly-NH₂ (SEQ ID NO: 147) Gly-His-Arg-Pro-Leu-Asp-Lys-L-Tic-Ile-Ser-Gly-Gly- Gly-Tyr-Arg-NH₂ (SEQ ID NO: 148) Gly-His-Arg-Pro-(SSS)-Oic-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 149) Gly-His-Arg-Pro-(SSS)1-aza-bicyclo[3.3.0]bicyclo- octan-carboxyl-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 150) Gly-His-Arg-Pro-Ala-cis-Acpc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 151) Gly-His-Arg-Pro-(1R, 2R)-Acpc-Ile-Ser-Gly-GlyNH₂ (SEQ ID NO: 152) Gly-His-Arg-Pro-Leu-(1S, 2S)-Acpc-Ile-Ser-Gly-Gly- NH₂ (SEQ ID NO: 153) Gly-His-Arg-Pro-Ile-(1-Acha)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 154) Gly-His-Arg-Pro-Acpo-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 155) Gly-His-Arg-Pro-(1-Acbc)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 156) Gly-His-Arg-Pro-Leu-Acpo-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 157) Gly-His-Arg-Pro-Ala-(1-Achc)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 158) Gly-His-Arg-Pro-((1R, 2S)-2-Achc)-Ile-Ser-Gly-Gly- NH₂ (SEQ ID NO: 159) Gly-His-Arg-Pro-Val-((1S, 2R)-2-Achc)-Ile-Ser-Gly- Gly-NH₂ (SEQ ID NO: 160) Gly-His-Arg-Pro-((1S, 2S)-2-Achc)-Ile-Ser-Gly-NH₂ (SEQ ID NO: 161) Gly-His-Arg-Pro-Leu-(1-Acpec)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 162) Gly-His-Arg-Pro-(1-Acprc)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 163) Gly-His-Arg-Pro-Aedfp-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 164) Gly-His-Arg-Pro-Val-(1-Aic)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 165) Gly-His-Arg-Pro-(2-Aic)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 166) Gly-His-Arg-Pro-LeuAmbc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 167) Gly-His-Arg-Pro-Ampa-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 168) Gly-His-Arg-Pro-Ile-Anc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 169) Gly-His-Arg-Pro-Atpc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 170) Gly-His-Arg-Pro-Ala-(2-Atc)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 171) Gly-His-Arg-Pro-Leu-Acbt-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 172) Gly-His-Arg-Pro-Acbo-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 173) Gly-His-Arg-Pro-Leu-(1-Acmb)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 174) Gly-His-Arg-Pro-Leu-(2-Acmb)-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 175) Gly-His-Arg-Pro-Acmv-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 176) Gly-His-Arg-Pro-Acq-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 177) Gly-His-Arg-Pro-Ala-Haic-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 178) Gly-His-Arg-Pro-Accb-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 179) Gly-His-Arg-Pro-Acpb-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 180) Gly-His-Arg-Pro-Leu-PBD-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 181) Gly-His-Arg-Pro-Ala-Bppp-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 182) Gly-His-Arg-Pro-Cptd-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 183) Gly-His-Arg-Pro-Leu-Thc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 184) Gly-His-Arg-Pro-Abhc-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 185) Gly-His-Arg-Pro-Ala-Accl-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 186) Gly-His-Arg-Pro-Leu-PLSP-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 187) Gly-His-Arg-Pro-BTD-Ile-Ser-Gly-Gly-NH₂ (SEQ ID NO: 188)

EXAMPLE 15

Gly-His-Arg-Pro-(1S, 2R)Achc-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 189)

The monomeric peptide is synthesized as in Example 1, Tentagel (Rapp Polymere) being used as resin support here with FMOC-Cys(Trt) as the first amino acid.

FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-(1S,2R)-Achc, and FMOC-Ser(tBu) (NeoMPS)

After cleavage and purification of the peptide reaction is carried out with a 2- to 8-fold molar excess of maleinimido-PEG_(20K). Following recovery purification is carried out on Kromasil RP-18, and the identity of the product is confirmed by way of analytical RP-HPLC and MALDI-MS.

EXAMPLE 16

Gly-His-Arg-Pro-Acdn-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 190)

The monomeric peptide is synthesized as in Example 1, Tentagel (Rapp Polymere) being used as resin support here with FMOC-Cys(Trt) as the first amino acid.

FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Acdn, and FMOC-Ser(tBu) (NeoMPS)

After cleavage and purification of the peptide reaction is carried out with a 2- to 8-fold molar excess of maleinimido-PEG_(20K). Following recovery purification is carried out on Kromasil RP-18, and the identity of the product is confirmed by way of analytical RP-HPLC and MALDI-MS.

Using the appropriate building blocks, the following peptide and peptidomimetic derivatives were prepared:

Gly-His-Arg-Pro-Pro-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 191) Gly-His-Arg-Pro-Leu-D-Pro-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide Gly-His-Arg-Pro-L-hydroxyproline-Ile-Ser-Gly-Gly- Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 192) Gly-His-Arg-Pro-D-hydroxproline-Ile-Ser-Gly-Gly- Cys-(S-succinimido-PEG_(20K))-amide Gly-His-Arg-Pro-Leu-L-(O-benzyl-hydroxyproline)- Ile-Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 193) Gly-His-Arg-Pro-D-(O-benzyl-hydroxyproline)-Ile- Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide Gly-His-Arg-Pro-Leu-L-(O-t-butyl-hydroxyproline)- Ile-Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 194) Gly-His-Arg-Pro-L-(O-2-naphtyl-hydroxyproline)- Ile-Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 195) Gly-His-Arg-Pro-Ala-L-(O-2-naphtyl-methyl-hydroxy- proline)-Ile-Ser-Gly-Gly-Cys-(S-succinimido- PEG_(20K))-amide (SEQ ID NO: 196) Gly-His-Arg-Pro-L-(O-phenyl-hydroxyproline)-Ile- Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 197) Gly-His-Arg-Pro-L-4-(4-pheny-benzyl-proline)-Ile- Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 198) Gly-His-Arg-Pro-Ala-L-(cis-3-phenyl-proline)-Ile- Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 199) Gly-His-Arg-Pro-L-(cis-4-phenyl-proline)-Ile-Ser- Gly-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 200) Gly-His-Arg-Pro-Ala-L-(trans-4-phenyl-proline)- Ile-Ser-Gly-Gly-Gly-Cys-(S-succinimido-PEG_(20K))- amide (SEQ ID NO: 201) Gly-His-Arg-Pro-L-(cis-5-phenyl-proline)-Ile-Ser- Gly-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 202) Gly-His-Arg-Pro-L-(trans-5-phenyl-proline)-Ile- Ser-Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 203) Gly-His-Arg-Pro-L-(4-benzyl-proline)-Ile-Ser-Gly- Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 204) Gly-His-Arg-Pro-Leu-L-(4-(4-bromobenzyl)-proline)- Ile-Ser-Gly-Gly-Gly-Cys-(S-succinimido-PEG_(20K))- amide (SEQ ID NO: 205) Gly-His-Arg-Pro-L-(4-cyclohexyl-proline)-Ile-Ser- Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 206) Gly-His-Arg-Pro-L-(4-fluoro-proline)-Ile-Ser-Gly- Gly-Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 207) Gly-His-Arg-Pro-Ala-L-Tic-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 208) Gly-His-Arg-Pro-(SSS)-Oic-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 209) Gly-His-Arg-Pro-(SSS)1-aza-bicyclo[3.3.0]bicyclo- octan-carboxyl-Ile-Ser-Gly-Cys-(S-succinimido- PEG_(20K))-amide (SEQ ID NO: 210) Gly-His-Arg-Pro-Ile-cis-Acpc-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 211) Gly-His-Arg-Pro-(1R, 2R)-Acpc-Ile-Ser-Gly-Gly-Cys- (S-succlnlmldo-PEG_(20K))-amide (SEQ ID NO: 212) Gly-His-Arg-Pro-(1S, 2S)-Acpc-Ile-Ser-Gly-Gly-Cys- (S-succlnlmldo-PEG_(20K))-amide (SEQ ID NO: 213) Gly-His-Arg-Pro-Leu-(1-Acha)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 214) Gly-His-Arg-Pro-Acpo-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 215) Gly-His-Arg-Pro-Leu-(1-Acbc)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 216) Gly-His-Arg-Pro-Acpo-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 217) Gly-His-Arg-Pro-Ala-(1-Achc)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 218) Gly-His-Arg-Pro-((1R, 2S)-2-Achc)-Ile-Ser-Gly-Gly- Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 219) Gly-His-Arg-Pro-Leu-((1S, 2R)-2-Achc)-Ile-Ser-Gly- Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 220) Gly-His-Arg-Pro-Ala-((1S, 2S)-2-Achc)-Ile-Ser-Gly- Gly-Cys-(S-succinimido-PEG_(20K))-amide (SEQ ID NO: 221) Gly-His-Arg-Pro-(1-Acpec)-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 222) Gly-His-Arg-Pro-(1-Acprc)-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 223) Gly-His-Arg-Pro-Leu-Aedfp-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 224) Gly-His-Arg-Pro-Leu-(1-Aic)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 225) Gly-His-Arg-Pro-Ala-(2-Aic)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 226) Gly-His-Arg-Pro-Ambc-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 227) Gly-His-Arg-Pro-Leu-Ampa-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 228) Gly-His-Arg-Pro-Anc-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 229) Gly-His-Arg-Pro-Leu-Atpc-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 230) Gly-His-Arg-Pro-Ile-(2-Atc)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 231) Gly-His-Arg-Pro-Acbt-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 232) Gly-His-Arg-Pro-Acbo-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 233) Gly-His-Arg-Pro-Ala-(1-Acmb)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 234) Gly-His-Arg-Pro-Lys-(2-Acmb)-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG_(20K))-amide (SEQ ID NO: 235) Gly-His-Arg-Pro-Leu-Acmv-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 236) Gly-His-Arg-Pro-Acq-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 237) Gly-His-Arg-Pro-Leu-Haic-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 238) Gly-His-Arg-Pro-Accb-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 239) Gly-His-Arg-Pro-Ala-Acpb-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 240) Gly-His-Arg-Pro-Leu-PBD-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 241) Gly-His-Arg-Pro-Bppp-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 242) Gly-His-Arg-Pro-Leu-Cptd-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 243) Gly-His-Arg-Pro-Thc-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 244) Gly-His-Arg-Pro-Leu-Abhc-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 245) Gly-His-Arg-Pro-Accl-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 246) Gly-His-Arg-Pro-Ala-PLSP-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 247) Gly-His-Arg-Pro-Leu-BTD-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG_(20K))-amide (SEQ ID NO: 248) Gly-His-Arg-Pro-(1S, 2R)Achc-Ile-Ser-Gly-Gly-Cys- (S-succinimido-PEG₃₀K)-amide (SEQ ID NO: 249) Gly-His-Arg-Pro-Leu-(1S, 2R)Achc-Ile-Ser-Gly-Gly- Cys-(S-succinimido-PEG₄₀K)-amide (SEQ ID NO: 250) Gly-His-Arg-Pro-Acdn-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG₃₀K)-amide (SEQ ID NO: 251) Gly-His-Arg-Pro-Acdn-Ile-Ser-Gly-Gly-Cys-(S- succinimido-PEG₄₀K)-amide (SEQ ID NO: 252)

EXAMPLE 17

The biological effect of the compounds was established in a model thrombin induced RhoA activation in human umbilical vein endothelial cell (HUVEC) culture.

HUVEC are grown to confluence under standard conditions. Before induction of Rho activity HUVEC were starved for 4 h by using IMDM (Gibco) without growth factor and serum supplements. After the starvation period 5 U/ml Thrombin (Calbiochem) or 5 U thrombin plus 50 μg/ml of test compound are added to the starvation medium for 1, 5 and 10 min. Active RhoA was isolated using Rho Assay Reagent from Upstate according to manufactures instructions. Isolates were separated on a 15% polyacrylamide gel and blotted on Nitrocellulose-Membrane (Bio-Rad). RhoA was detected by using Anti-Rho (-A, -B, -C), clone55 from Upstate (1:500).

Relative RhoA stimulation compared to unstimulated control

Control peptide 1 min 1 Control peptide 5 min 1 Control peptide 10 min 1 thrombin 5 min 6.2 thrombin + compound example 1 (10 min) 2.2 

1. A compound of the general formula II H₂N-GHRPX₁-β-X₄X₅GGX₈X₉X₁₀-X₁₁ (SEQ ID NO: 2) (II),

or a physiologically acceptable salt thereof, wherein X₁ denotes L, I, A or is absent, X₄ denotes L, I, S, M or A, and X₅ denotes A, G, S, or L, or X₄ X₅ jointly denote a spacer of a length similar to 2 amino acids in chain length, X₈ denotes a genetically coded amino acid or is absent, X₉ denotes a genetically coded amino acid or is absent, X₁₀ denotes a genetically coded amino acid or is absent, X₁₁ denotes OR₁, wherein R₁ is hydrogen or (C₁-C₁₀)alkyl, NR₂R₃ with R₂ and R₃ being identical or different and denoting hydrogen, (C₁-C₁₀)alkyl or W-PEG_(5-60K), wherein PEG is attached via a spacer W to the N-atom of NR₂R₃, or Y-Z-PEG_(5-60K), wherein Y denotes a genetically coded amino acid selected from the group S, C, K or R, or is absent, and wherein Z denotes a spacer, via which polyethylene glycol (PEG) can be attached, and β denotes a genetically coded amino acid, a non-naturally occurring amino acid, or a peptidomimetic element, which induces a bend or turn in the peptide backbone of general formula II.
 2. The compound of claim 1, wherein β is selected from the following: L-proline, D-L-proline, D-proline, L-hydroxyproline, D-hydroxyproline, L-(O -benzyl)-hydroxyproline, D-(O-benzyl)-hydroxyproline, L-(O-tert.butyl)-hydroxyproline, 4-(O-2-naphtyl)-hydroxyproline, 4-(O-2-naphtyl-methyl)-hydroxyproline, 4-(O-phenyl)- hydroxyproline, 4-(4-phenyl-benzyl)-proline, cis-3-phenyl-proline, cis-4-phenyl-proline, trans-4-phenyl-proline, cis-5-phenyl-proline, trans-5-phenyl-proline, 4-benzyl-proline, 4-bromobenzyl-proline, 4-cyclohexyl-proline, 4-fluor-proline, L-tetrahydroisoquinoline-2-carboxylic acid (L-Tic), a diastereomer of octahydro-indole-2-carboxylic acid (Oic), a diastereomer of 1-aza-bicyclo[3,3,0]octane-2-carboxylic acid,

cis-2-aminocyclopentane carboxylic acid (cis-Acpc)

(1R,2R)-(2-aminocyclopentane carboxylic acid ((1R,2R)-Acpc)

(1S,2S)-(2-aminocyclopentane carboxylic acid ((1S,2S)-Acpc)

1-aminomethyl-cyclohexane acetic acid (1-Achc)

3-amino-1-carboxymethyl-pyridin-2-one (Acpo)

1-amino-cyclobutane-carboxylic acid (1-Acbc)

1-amino-cyclohexane-carboxylic acid (1-Achc)

cis-4-amino-cyclohexane-acetic acid (4-Acha)

(1R,2R)-2-aminocyclohexane carboxylic acid ((1R,2R)-Achc)

(1R,2S)-2-aminocyclohexane carboxylic acid ((1R,2S)-Achc)

(1S,2R)-2-aminocyclohexane carboxylic acid ((1S,2R)-Achc)

(1S,2S)-2-aminocyclohexane carboxylic acid ((1S,2S)-Achc)

1-amino-cyclopentane carboxylic acid (1-Acpec)

1-amino-cyclopropane carboxylic acid (1-Acprc)

4-(2-aminoethyl)-6-dibenzofuranpropionic acid (Aedfp)

(R,S)-1-aminoindane-1-carboxylic acid (1-Aic)

2-aminoindane-2-carboxylic acid (2-Aic)

2′-(aminomethyl)-biphenyl-2-carboxylic acid (Ambc)

2-aminomethyl-phenylacetic acid (Ampa)

3-amino-2-naphthoic acid (Anc)

4-amino-tetrahydropyran-4-carboxylic acid (Atpc)

(R,S)-2-aminotetraline-2-carboxylic acid (2-Atc)

(2S,6S,9S)-6-amino-2-carboxymethyl-3,8- diazabicyclo-[4,3,0]-nonane-1,4-dione (Acdn)

(R)-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (Acbt)

(S)-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (Acbt)

(R,S)-3-amino-1-carboxymethyl-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one (1-Acmb)

(S)-4-amino-2-carboxymethyl-1,3,4,5-tetrahydro-2H-[2]-benzazepin-3-one (2-Acmb)

(R,S)-3-amino-1-carboxymethyl-valerolactame (Acmv)

3-(2-aminoethyl)-1-carboxymethyl-quinazoline-2,4- dione (Acq)

(2S,5S)-5-amino-1,2,4,5,6,7-hexahydro-azepino [3,2,1-hi]-indole-4-one-2-carboxylic acid (Haic)

(R,S)-3-amino-N-1-carboxymethyl-2-oxo-5-cyclohexyl-1,4-benzodiazepine (Accb)

(R,S)-3-amino-N-1-carboxymethyl-2-oxo-5-phenyl-1,4-benzodiazepine (Acpb)

(2S,11aS)-2-amino-10-carboxymethyl-1,2,3,11 a-tetrahydro-10OH-pyrrolo[2,1-c][1,4]-benzodiazepine-5,11-dione (PBD)

(2S,3′S)-2-(4′-(3′-benzyl-2′-oxo-piperazin-1-yl))-3-phenyl-propionic acid (Bppp)

3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (Cptd)

(R,S)-3-amino-9-Boc-1,2,3,4-tetrahydro-carbazole-3-carboxylic acid (Thc)

3-exo-amino-bicyclo[2.2.1]heptane-2-exo-carboxylic acid (Abhc)

(3S)-3-amino-1-carboxymethyl-caprolactam (Accl)

(S,S)-(ProLeu)spirolactame (PLSP) and

2-oxo-3-amino-7-thia-1-azabicyclo[4.3.0]nonane-9-carcoxylich acid (BTD).
 3. The compound of claim 1, wherein: X₄ denotes L, I, S, M or A, and X₅ denotes A, G, S, or L.
 4. The compound of claim 1, wherein: X₄ denotes I, and X₅ denotes S.
 5. The compound of claim 1, wherein: X₁ is absent.
 6. The compound of claim 1, wherein: X₈ is absent, X₉ is absent, and X₁₀ is absent.
 7. The compound of claim 1, wherein: β is:

cis-4-amino-cyclohexane-acetic acid (4-Acha).
 8. The compound of claim 1, wherein: X₁ is absent. X₄ denotes I, X₅ denotes S, X₈ is absent, X₉ is absent, X₁₀ is absent. β is

cis-4-amino-cyclohexane-acetic acid (4-Acha), and X₁₁ denotes OR₁ wherein R₁ is hydrogen.
 9. A pharmaceutical composition comprising the compound of claim
 1. 10. A pharmaceutical composition comprising the compound of claim
 8. 